A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6201410



Internal ID9792078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:51628786..51630486hg38UCSC Ensembl
Outerchr1:51628629..51630639hg38UCSC Ensembl
Innerchr1:52094458..52096158hg19UCSC Ensembl
Outerchr1:52094301..52096311hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg382011
hg192011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676547
Supporting Variants
SamplesNA19785
Known GenesOSBPL9
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6201410
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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